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FDA 510(k)

AMK LANDMARK REVISION KNEE SYSTEM

K-Number: K925072 · 1994-01-21

ApplicantDepuy, Inc.
Decision Date1994-01-21
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AMK LANDMARK REVISION KNEE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1994-01-21 under 510(k) number K925072. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMK LANDMARK REVISION KNEE SYSTEM?

AMK LANDMARK REVISION KNEE SYSTEM is a medical device that received FDA 510(k) clearance on 1994-01-21. The listed applicant is Depuy, Inc.. The 510(k) number is K925072.

When did AMK LANDMARK REVISION KNEE SYSTEM receive FDA 510(k) clearance?

AMK LANDMARK REVISION KNEE SYSTEM received FDA 510(k) clearance on 1994-01-21, under 510(k) number K925072.

Who is the listed applicant for AMK LANDMARK REVISION KNEE SYSTEM?

The FDA 510(k) record lists Depuy, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMK LANDMARK REVISION KNEE SYSTEM?

The FDA product code for AMK LANDMARK REVISION KNEE SYSTEM is JWH.

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Related Devices (Code: JWH)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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